• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Lower Annual Rate of Progression of Short-Segment vs Long-Segment Barrett's Esophagus to Esophageal Adenocarcinoma.短节段 Barrett 食管与长节段 Barrett 食管进展为食管腺癌的年发生率较低。
Clin Gastroenterol Hepatol. 2019 Apr;17(5):864-868. doi: 10.1016/j.cgh.2018.07.008. Epub 2018 Aug 8.
2
Significantly lower annual rates of neoplastic progression in short- compared to long-segment non-dysplastic Barrett's esophagus: a systematic review and meta-analysis.与长节段非异型增生性 Barrett 食管相比,短节段非异型增生性 Barrett 食管的肿瘤进展年发生率显著降低:系统评价和荟萃分析。
Endoscopy. 2019 Jul;51(7):665-672. doi: 10.1055/a-0869-7960. Epub 2019 Apr 2.
3
Association between length of Barrett's esophagus and risk of high-grade dysplasia or adenocarcinoma in patients without dysplasia.巴雷特食管长度与无异型增生患者高级别异型增生或腺癌风险的关系。
Clin Gastroenterol Hepatol. 2013 Nov;11(11):1430-6. doi: 10.1016/j.cgh.2013.05.007. Epub 2013 May 22.
4
Development and Validation of a Model to Determine Risk of Progression of Barrett's Esophagus to Neoplasia.发展和验证一个模型以确定 Barrett 食管进展为肿瘤的风险。
Gastroenterology. 2018 Apr;154(5):1282-1289.e2. doi: 10.1053/j.gastro.2017.12.009. Epub 2017 Dec 19.
5
Incidence of Progression of Persistent Nondysplastic Barrett's Esophagus to Malignancy.持续性非异型增生 Barrett 食管进展为恶性肿瘤的发生率。
Clin Gastroenterol Hepatol. 2019 Apr;17(5):869-877.e5. doi: 10.1016/j.cgh.2018.08.033. Epub 2018 Sep 11.
6
Patients with nondysplastic Barrett's esophagus have low risks for developing dysplasia or esophageal adenocarcinoma.非异型增生性 Barrett 食管患者发生异型增生或食管腺癌的风险较低。
Clin Gastroenterol Hepatol. 2011 Mar;9(3):220-7; quiz e26. doi: 10.1016/j.cgh.2010.11.008. Epub 2010 Nov 27.
7
Dysplasia in short-segment Barrett's esophagus: a prospective 3-year follow-up.短节段巴雷特食管的发育异常:一项为期3年的前瞻性随访研究
Am J Gastroenterol. 1997 Nov;92(11):2012-6.
8
Increasing prevalence of high-grade dysplasia and adenocarcinoma on index endoscopy in Barrett's esophagus over the past 2 decades: data from a multicenter U.S. consortium.过去 20 年中,巴雷特食管在内窥镜下高级别异型增生和腺癌的检出率不断增加:来自美国多中心联盟的数据。
Gastrointest Endosc. 2019 Feb;89(2):257-263.e3. doi: 10.1016/j.gie.2018.09.041. Epub 2018 Oct 17.
9
Low Risk of High-Grade Dysplasia or Esophageal Adenocarcinoma Among Patients With Barrett's Esophagus Less Than 1 cm (Irregular Z Line) Within 5 Years of Index Endoscopy.在索引内镜检查后 5 年内,食管直径小于 1 厘米(不规则 Z 线)的 Barrett 食管患者发生高级别异型增生或食管腺癌的风险较低。
Gastroenterology. 2017 Apr;152(5):987-992. doi: 10.1053/j.gastro.2016.12.005. Epub 2016 Dec 15.
10
Risk of malignant progression in Barrett's esophagus indefinite for dysplasia.巴雷特食管不典型增生不能确定时的恶性进展风险
Dis Esophagus. 2017 Mar 1;30(3):1-5. doi: 10.1093/dote/dow025.

引用本文的文献

1
EsoDetect: computational validation and algorithm development of a novel diagnostic and prognostic tool for dysplasia in Barrett's esophagus.EsoDetect:一种用于巴雷特食管发育异常的新型诊断和预后工具的计算验证与算法开发
PeerJ. 2025 Jul 3;13:e19613. doi: 10.7717/peerj.19613. eCollection 2025.
2
A Clinical Validation of a Diagnostic Test for Esophageal Adenocarcinoma Based on a Novel Serum Glycoprotein Biomarker Panel: PromarkerEso.基于新型血清糖蛋白生物标志物组合PromarkerEso的食管腺癌诊断测试的临床验证
Proteomes. 2025 Jun 4;13(2):23. doi: 10.3390/proteomes13020023.
3
Carcinoma of Esophagus.食管癌
J Gastroenterol Hepatol. 2025 Aug;40(8):1861-1875. doi: 10.1111/jgh.16990. Epub 2025 Jun 24.
4
A Simple, Interpretable Machine Learning Model Based on Clinical Factors Accurately Predicts Incident Dysplasia or Malignancy in Barrett's Esophagus.一种基于临床因素的简单、可解释的机器学习模型能够准确预测巴雷特食管的异型增生或恶性病变。
Dig Dis Sci. 2025 Apr 28. doi: 10.1007/s10620-025-09069-w.
5
The Tissue Systems Pathology Test Objectively Risk-Stratifies Patients With Barrett's Esophagus: Results From a Multicenter US Clinical Experience Study.组织系统病理学检测可客观地对巴雷特食管患者进行风险分层:一项美国多中心临床经验研究的结果
J Clin Gastroenterol. 2025 Jul 1;59(6):531-536. doi: 10.1097/MCG.0000000000002040.
6
Understanding the malignant potential of gastric metaplasia of the oesophagus and its relevance to Barrett's oesophagus surveillance: individual-level data analysis.了解食管胃型化生的恶性潜能及其与 Barrett 食管监测的相关性:个体水平数据分析。
Gut. 2024 Apr 5;73(5):729-740. doi: 10.1136/gutjnl-2023-330721.
7
Perioperative Interventions to Prevent Gastroesophageal Reflux Disease and Marginal Ulcers After Bariatric Surgery - an International Experts' Survey.减重手术后预防胃食管反流病和边缘性溃疡的围手术期干预措施 - 国际专家调查。
Obes Surg. 2023 May;33(5):1449-1462. doi: 10.1007/s11695-023-06481-x. Epub 2023 Feb 13.
8
High rate of missed Barrett's esophagus when screening with forceps biopsies.食管钳活检筛查时漏诊 Barrett 食管的比例较高。
Esophagus. 2023 Jan;20(1):143-149. doi: 10.1007/s10388-022-00943-4. Epub 2022 Jul 22.
9
Effect of gastro-esophageal reflux symptoms on the risk of Barrett's esophagus: A systematic review and meta-analysis.胃食管反流症状对 Barrett 食管风险的影响:系统评价和荟萃分析。
J Gastroenterol Hepatol. 2022 Aug;37(8):1507-1516. doi: 10.1111/jgh.15902. Epub 2022 Jun 2.
10
Endoscopic diagnosis and screening of Barrett's esophagus: Inconsistency of diagnostic criteria between Japan and Western countries.巴雷特食管的内镜诊断与筛查:日本与西方国家诊断标准的不一致性。
DEN Open. 2021 Nov 15;2(1):e73. doi: 10.1002/deo2.73. eCollection 2022 Apr.

本文引用的文献

1
ACG Clinical Guideline: Diagnosis and Management of Barrett's Esophagus.美国胃肠病学会临床指南:巴雷特食管的诊断与管理
Am J Gastroenterol. 2016 Jan;111(1):30-50; quiz 51. doi: 10.1038/ajg.2015.322. Epub 2015 Nov 3.
2
Length of Barrett's oesophagus and cancer risk: implications from a large sample of patients with early oesophageal adenocarcinoma.巴雷特食管长度与癌症风险:来自一大群早期食管腺癌患者的启示。
Gut. 2016 Feb;65(2):196-201. doi: 10.1136/gutjnl-2015-309220. Epub 2015 Jun 25.
3
Barrett's oesophagus length is established at the time of initial endoscopy and does not change over time: results from a large multicentre cohort.巴雷特食管的长度在初次内镜检查时确定,且不会随时间改变:一项大型多中心队列研究结果。
Gut. 2015 Dec;64(12):1874-80. doi: 10.1136/gutjnl-2014-308552. Epub 2015 Feb 4.
4
Surveillance in patients with long-segment Barrett's oesophagus: a cost-effectiveness analysis.长段 Barrett 食管患者的监测:成本效益分析。
Gut. 2015 Jun;64(6):864-71. doi: 10.1136/gutjnl-2014-307197. Epub 2014 Jul 18.
5
British Society of Gastroenterology guidelines on the diagnosis and management of Barrett's oesophagus.英国胃肠病学会 Barrett 食管诊断和管理指南。
Gut. 2014 Jan;63(1):7-42. doi: 10.1136/gutjnl-2013-305372. Epub 2013 Oct 28.
6
Association between length of Barrett's esophagus and risk of high-grade dysplasia or adenocarcinoma in patients without dysplasia.巴雷特食管长度与无异型增生患者高级别异型增生或腺癌风险的关系。
Clin Gastroenterol Hepatol. 2013 Nov;11(11):1430-6. doi: 10.1016/j.cgh.2013.05.007. Epub 2013 May 22.
7
The incidence of oesophageal adenocarcinoma in non-dysplastic Barrett's oesophagus: a meta-analysis.非异型增生性 Barrett 食管中食管腺癌的发病率:一项荟萃分析。
Gut. 2012 Jul;61(7):970-6. doi: 10.1136/gutjnl-2011-300730. Epub 2011 Oct 13.
8
Incidence of adenocarcinoma among patients with Barrett's esophagus.巴雷特食管患者腺癌的发病率。
N Engl J Med. 2011 Oct 13;365(15):1375-83. doi: 10.1056/NEJMoa1103042.
9
Risk of malignant progression in Barrett's esophagus patients: results from a large population-based study.巴雷特食管患者恶性进展的风险:一项大型基于人群的研究结果。
J Natl Cancer Inst. 2011 Jul 6;103(13):1049-57. doi: 10.1093/jnci/djr203. Epub 2011 Jun 16.
10
American Gastroenterological Association medical position statement on the management of Barrett's esophagus.美国胃肠病学会关于巴雷特食管管理的医学立场声明。
Gastroenterology. 2011 Mar;140(3):1084-91. doi: 10.1053/j.gastro.2011.01.030.

短节段 Barrett 食管与长节段 Barrett 食管进展为食管腺癌的年发生率较低。

Lower Annual Rate of Progression of Short-Segment vs Long-Segment Barrett's Esophagus to Esophageal Adenocarcinoma.

机构信息

Gastroenterology and Hepatology, University of Kansas Medical Center, Kansas City, Kansas; Gastroenterology and Hepatology, Veterans Affairs Medical Center, Kansas City, Missouri.

Gastroenterology and Hepatology, Veterans Affairs Medical Center, Kansas City, Missouri.

出版信息

Clin Gastroenterol Hepatol. 2019 Apr;17(5):864-868. doi: 10.1016/j.cgh.2018.07.008. Epub 2018 Aug 8.

DOI:10.1016/j.cgh.2018.07.008
PMID:30012433
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7050470/
Abstract

BACKGROUND & AIMS: European guidelines recommend different surveillance intervals of non-dysplastic Barrett's esophagus (NDBE) based on segment length, as opposed to guidelines in the United States, which do recommend surveillance intervals based on BE length. We studied rates of progression of NDBE to high-grade dysplasia (HGD) or esophageal adenocarcinoma (EAC) in patients with short-segment BE using the definition of BE in the latest guidelines (length ≥1 cm).

METHODS

We collected demographic, clinical, endoscopy, and histopathology data from 1883 patients with endoscopic evidence of NDBE (mean age, 57.3 years; 83.5% male; 88.1% Caucasians) seen at 7 tertiary referral centers. Patients were followed for a median 6.4 years. Cases of dysplasia or EAC detected within 1 year of index endoscopy were considered prevalent and were excluded. Unadjusted rates of progression to HGD or EAC were compared between patients with short (≥1 and <3) and long (≥3) BE lengths using log-rank tests. A subgroup analysis was performed on patients with a documented Prague C&M classification. We used a multivariable proportional hazards model to evaluate the association between BE length and progression. Adjusted hazards ratios were calculated after adjusting for variables associated with progression.

RESULTS

We found 822 patients to have a short-segment BE (SSBE) and 1061 to have long segment BE (LSBE). We found patients with SSBE to have a significantly lower annual rate of progression to EAC (0.07%) than of patients with LSBE (0.25%) (P = .001). For the combined endpoint of HGD or EAC, annual progression rates were significantly lower among patients with SSBE (0.29%) compared to compared to LSBE (0.91%) (P < .001). This effect persisted in multivariable analysis (hazard ratio, 0.32; 95% CI, 0.18-0.57; P < .001).

CONCLUSION

We analyzed progression of BE (length ≥1 cm) to HGD or EAC in a large cohort of patients seen at multiple centers and followed for a median 6.4 years. We found a lower annual rate of progression of SSBE to EAC (0.07%/year) than of LSBE (0.25%/year). We propose lengthening current surveillance intervals for patients with SSBE.

摘要

背景与目的

欧洲指南根据节段长度建议不同的非异型性 Barrett 食管(NDBE)监测间隔,而美国指南则根据 BE 长度建议监测间隔。我们使用最新指南(长度≥1 cm)中 BE 的定义,研究了短节段 BE 患者(NDBE)进展为高级别异型增生(HGD)或食管腺癌(EAC)的比率。

方法

我们收集了 7 家三级转诊中心内镜检查发现的 1883 例 NDBE 患者的人口统计学、临床、内镜和组织病理学数据(平均年龄 57.3 岁;83.5%为男性;88.1%为白种人)。中位随访时间为 6.4 年。索引内镜检查后 1 年内发现的异型增生或 EAC 病例被视为现患病例,并予以排除。使用对数秩检验比较短(≥1 且<3)和长(≥3)BE 长度患者之间进展为 HGD 或 EAC 的未调整率。对有记录的布拉格 C&M 分类的患者进行了亚组分析。我们使用多变量比例风险模型评估 BE 长度与进展之间的关系。在调整与进展相关的变量后,计算调整后的危险比。

结果

我们发现 822 例患者存在短节段 BE(SSBE),1061 例患者存在长节段 BE(LSBE)。与 LSBE 患者(0.25%)相比,SSBE 患者的 EAC 年进展率(0.07%)显著较低(P=0.001)。对于 HGD 或 EAC 的联合终点,SSBE 患者的年进展率(0.29%)明显低于 LSBE 患者(0.91%)(P<0.001)。多变量分析结果一致(风险比,0.32;95%CI,0.18-0.57;P<0.001)。

结论

我们分析了多个中心就诊的大量患者的 BE(长度≥1 cm)进展为 HGD 或 EAC 的情况,并进行了中位 6.4 年的随访。我们发现 SSBE 进展为 EAC 的年发生率(0.07%/年)低于 LSBE(0.25%/年)。我们建议延长 SSBE 患者的当前监测间隔。